Department of Health and Social Care written question – answered at on 27 June 2022.
To ask the Secretary of State for Health and Social Care, with reference to the Answer of 20 April 2022 to Question 151279, on Evusheld, whether the UKHSA has reviewed studies published by the US Food and Drug Administration and European Medicines Agency on the effectiveness of Evusheld against the covid-19 omicron variant; and for what reason the UKHSA has decided to undertake duplicate studies on the effectiveness of that drug.
The UK Health Security Agency has been commissioned by AstraZeneca to undertake specific testing on the efficacy of Evusheld and therefore has no plans to review external studies. UKHSA began the process of testing against the Omicron variant in March 2022. Following the completion of preliminary laboratory work, such testing lasts for approximately three to four weeks. The data gathered will be considered by expert clinical groups with other available information, which will inform any potential procurement decisions.
Yes3 people think so
No37 people think not
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